Multicentre, randomised controlled feasibility study to compare a 10-week physiotherapy programme using an interactive exercise training device to improve walking and balance, to usual care of children with cerebral palsy aged 4-18 years: the ACCEPT study protocol

被引:4
作者
Rapson, Rachel [1 ,2 ]
Marsden, Jonathan [3 ]
Latour, Jos [4 ]
Ingram, Wendy [5 ]
Stevens, Kara Nicola [6 ]
Cocking, Laura [7 ]
Carter, Bernie [8 ]
机构
[1] Torbay & South Devon Natl Hlth Serv Fdn Trust, Children & Family Hlth Devon, Physiotherapy, Torquay, England
[2] Univ Plymouth, Fac Hlth & human Sci, Plymouth, Devon, England
[3] Univ Plymouth, Fac Hlth & Human Sci, Plymouth, Devon, England
[4] Univ Plymouth, Sch Nursing & Midwifery, Plymouth, Devon, England
[5] Plymouth Univ, Peninsula Sch Med & Dent, Peninsula Clin Trials Unit, Plymouth, Devon, England
[6] Univ Plymouth, Med Stat, Plymouth, Devon, England
[7] Univ Plymouth, Plymouth Univ PenCTU, Peninsula Clin Trials Unit, Plymouth, Devon, England
[8] Edge Hill Univ, Fac Hlth & Social Care, Ormskirk, England
来源
BMJ OPEN | 2022年 / 12卷 / 05期
关键词
Paediatric neurology; REHABILITATION MEDICINE; Developmental neurology & neurodisability; GROSS MOTOR FUNCTION; PERFORMANCE;
D O I
10.1136/bmjopen-2021-058916
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Children with cerebral palsy (CP) frequently undertake physiotherapy programmes to improve walking and balance. They often require adult support to exercise in a functional position. A novel interactive exercise trainer has been devised to enable children to exercise with against resistance in a functional position, but its efficacy has yet to be proved. A novel protocol has been developed to determine whether a randomised controlled trial (RCT) is feasible. Aim To establish whether it is feasible to conduct an RCT to assess the effectiveness of a 10-week physiotherapy intervention using an interactive trainer in children with CP. Methods and analysis This study is multicentre randomised controlled feasibility trial with an embedded qualitative study. Forty children with CP, Gross Motor Function Classification System (GMFCS) I-III will be recruited from community paediatric physiotherapy caseloads. Participants will be randomised to 10 weeks of training with the interactive training device or to usual physiotherapy care. The mediolateral motion of the centre of mass estimate and Paediatric Balance Scale will be explored as potential primary outcomes measures, tested at baseline, 10 weeks and follow-up at 20 weeks. The views of child participants, their parents and physiotherapists will be gained through e-diaries and qualitative interviews. Feasibility will be determined by examining recruitment and retention rates, completeness of, adherence to the intervention, appropriateness of outcome measures and effectiveness of blinding. Results will be reported in accordance to Consolidated Standards of Reporting Trials (CONSORT) guidelines. Ethics and dissemination Physiotherapists, children and parents have informed trial design and information leaflets. Results will be disseminated via publications, conferences and to families. This study has approval from North of Scotland Research Ethics Committee (20/NS/0018).
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页数:7
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